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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37039생성일: 2026년 10월 24일

Trityl chloride → N-triphenylmethyl-alpha-aminobutyrolactone

https://huagongshe.com/ko/reaction/37039

반응식

참여 물질

역할이름HCID투입량
반응물Trityl chlorideHCID 6456—
반응물4-MethylmorpholineHCID 7972—
반응물Homoserine lactone hydrobromideHCID 73508—
용매DimethylformamideHCID 6228—
생성물N-triphenylmethyl-alpha-aminobutyrolactoneHCID 13856082—

반응 단계

α-Aminobutyrolactone hydrobromide (10.0 g, 54.9 mmol), N-methylmorpholine (11.2 g, 110.0 mmol) and triphenylmethyl chloride (15.4 g, 55.2 mmol) were dissolved in N,N-dimethylformamide (DMF) (200 ml) (distilled from calcium hydride) and stirred at ambient temperature for 16 hours. The mixture was filtered, and water (200 ml) was added to the DMF-solution. The resulting slurry was stirred for 2 hours, the precipitate was filtered off and washed with a mixutre of DMF and water (1:1, 50 ml). The solid was resuspended in water (100 ml), filtered and dried at 50° C. in vacuo. N-triphenylmethyl-α-amino-butyrolactone was isolated as a white solid. Yield 17.55 g (93.2%), mp 164.5°-165.5° C. (uncorrected).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05419893
출처 데이터셋uspto-grants-1995_05
ORD IDord-53b464ac8a92404eaf0cf1fbc086b494
출처 메모uspto-grants-1995_05